RPGRIP1L polyclonal antibody
产品名称： RPGRIP1L polyclonal antibody
英文名称： RPGRIP1L polyclonal antibody
产品编号： PAB7600
产品价格： null
产品产地： 台湾
品牌商标： Abnova
更新时间： null
使用范围：
亚诺法生技股份有限公司（Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Goat polyclonal antibody raised against synthetic peptide of RPGRIP1L.
- Immunogen:
- A synthetic peptide corresponding to human RPGRIP1L.
- Sequence:
- C-DKENNKAKRDILK
- Host:
- Goat
- Theoretical MW (kDa):
- 151
- Reactivity:
- Human
- Form:
- Liquid
- Purification:
- Antigen affinity purification
- Concentration:
- 0.5 mg/mL
- Storage Buffer:
- In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
- Storage Instruction:
- Store at -20°C.
Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Synthetic Peptide.
- Recommend Usage:
- ELISA (1:64000)
Western Blot (0.3-1 ug/mL)
The optimal working dilution should be determined by the end user.
- Note:
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Publication Reference
- 1.
- Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.
Arts HH, Doherty D, van Beersum SE, Parisi MA, Letteboer SJ, Gorden NT, Peters TA, Marker T, Voesenek K, Kartono A, Ozyurek H, Farin FM, Kroes HY, Wolfrum U, Brunner HG, Cremers FP, Glass IA, Knoers NV, Roepman R.Nat Genet. 2007 Jul;39(7):882-8. Epub 2007 Jun 10.
- Entrez GeneID:
- 23322
- Protein Accession#:
- NP_056087.2
- Gene Name:
- RPGRIP1L
- Gene Alias:
- CORS3,DKFZp686C0668,JBTS7,KIAA1005,MKS5,NPHP8
- Gene Description:
- RPGRIP1-like
- Omim ID:
- 610937
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
- Other Designations:
- RPGR-interacting protein 1-like protein,protein fantom